rs876661231

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs876661231(G;T)

Make rs876661231(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

95172105

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs876661231
dbSNP (classic)	rs876661231
ClinGen	rs876661231
ebi	rs876661231
HLI	rs876661231
Exac	rs876661231
Gnomad	rs876661231
Varsome	rs876661231
LitVar	rs876661231
Map	rs876661231
PheGenI	rs876661231
Biobank	rs876661231
1000 genomes	rs876661231
hgdp	rs876661231
ensembl	rs876661231
geneview	rs876661231
scholar	rs876661231
google	rs876661231
pharmgkb	rs876661231
gwascentral	rs876661231
openSNP	rs876661231
23andMe	rs876661231
SNPshot	rs876661231
SNPdbe	rs876661231
MSV3d	rs876661231
GWAS Ctlg	rs876661231

Max Magnitude

0

ClinVar
Risk	rs876661231(T;T)
Alt	rs876661231(T;T)
Reference	Rs876661231(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FANCC
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.97934387C>A
CLNSRC
CLNACC	RCV000219758.1,